Antibacterial penicillins

ABSTRACT

This invention relates to a new class of penicillins (I) and their pharmaceutically acceptable salts and esters which are useful as antibiotics: ##STR1## wherein the stylized radical (hereafter referred to as R&#39;): ##STR2## represents a mono- or polycyclic N-containing heterocyclic group; R 2  is H or OH; and R is, inter alia, hydrogen, substituted and unsubstituted: alkyl, aryl, alkenyl, heterocyclylalkyl, heterocyclylalkenyl, aralkyl, aralkenyl, --NR 2 , --COOR, CONR 2 , --OR or CN.

BACKGROUND OF THE INVENTION

This invention relates to a new class of penicillins (I) and their pharmaceutically acceptable salts and esters which are useful as antibiotics: ##STR3## wherein the stylized radical (hereafter referred to as R'): ##STR4## represents a mono- or polycyclic N-containing heterocyclic group; R² is H or OH; and

R is, inter alia, hydrogen, substituted and unsubstituted: alkyl, aryl, alkenyl, heterocyclylalkyl, heterocyclylalkenyl, aralkyl, aralkenyl, --NR₂, COOR, CONR₂, --OR, or CN. The heterocyclic radical R' is further defined below.

This invention also relates to processes for the preparation of such compounds (I); pharmaceutical compositions comprising such compounds; and to methods of treatment comprising administering such compounds and compositions when an antibiotic effect is indicated.

There is a continuing need for new antibiotics. For unfortunately, there is no static effectiveness of any given antibiotic because continued wide scale usage selectively gives rise to resistant strains of pathogens. In addition, the known antibiotics suffer from the disadvantage of being effective only against certain types of microorganisms. Accordingly, the search for new antibiotics continues.

Thus, it is an object of the present invention to provide a novel class of antibiotics which are useful in animal and human therapy and in inanimate systems. These antibitoics are active against a broad range of pathogens which representatively include both gram positive bacteria such as S. aureus, Strep. pyogenes, and B. subtilis, and gram negative bacteria such as E. coli, Pseudomonas, Proteus morganii, Serratia, and Klebsiella. Further objects of this invention are to provide chemical processes for the preparation of such antibiotics and their non-toxic pharmaceutically acceptable salts and esters; pharmaceutical compositions comprising such antibiotics; and to provide methods of treatment comprising administering such antibiotics and compositions when an antibiotic effect is indicated.

DETAILED DESCRIPTION OF THE INVENTION

The compounds of the present invention are prepared by reacting an appropriately substituted 6-(α-aminoacyl)aminopenicillanic acid (1) with a chosen electrophilic N-heterocyclic reagent (2 or 3) calculated to provide the species of the present invention I. The following reaction diagram conveniently summarizes this process and introduces the precise identity of such electrophilic reagents and the nature of the products of this reaction (I, above). ##STR5## wherein: B is, inter alia, the residue of a 5-, or a 6-membered aromatic heterocycle; or a 5,5-, 6,5-; or 6,6-bicyclic aromatic heterocycle; wherein the additional ring atoms are chosen either entirely as carbon, or include one or more atoms selected from S, N and O. The carbon and nitrogen atoms of any such ring may carry substituents such as substituted and unsubstituted: alkyl and alkenyl having 1-6 carbon atoms, phenyl, phenylalkyl having 1-6 carbon atoms in the alkyl moiety, 5- or 6-membered heterocyclyl wherein the hetero atom or atoms are selected from O, N or S, --OR₂, --NR₂, --COOR, --CONR₂, --CN, halo, --SR, 13 SO.R₃, --SO₂ R, --NHCONH₂, --SO₃ R, --SO₂ NR₂ (R is defined immediately below), ##STR6## R° is hydrogen or alkyl having 1-6 carbon atoms); wherein the substituent or substituents are selected from halogen such as chlorine or fluorine, hydroxyl, phenyl, alkyl, alkoxyl, carboxyl and phenylalkyl (each alkyl having 1-6 carbon atoms);

R is selected from H; substituted and unsubstituted: alkyl having 1-10 carbon atoms, alkenyl having 2-10 carbon atoms, phenyl, phenylalkyl, phenylalkenyl having 7-12 carbon atoms, 5-or 6-membered heterocyclylalkyl wherein the hetero atom or atoms are selected from O, N or S and the alkyl has 1-6 carbon atoms, NR₂, OR, COOR, CN, and CONR₂ (R is defined here); wherein the substituent or substituents on R are selected from halogen such as chloro and fluoro, hydroxyl, OR, NR₂, COOR, CONR₂, CN, ##STR7## --SR, --SO.R, --SO₂ R, (R° is hydrogen or alkyl having 1-6 carbon atoms), and alkyl having 1-6 carbon atoms;

R and B together may be joined to yield 6.5- and 6,6-bicyclic heterocycles in which the N.sup.⊕ is at a bridgehead;

X is a leaving group such as halogen, preferably fluorine; other leaving groups include: OCH₃, SCH₃ ; OSO₂ OCH₃ OSO₂ OCF₃, ##STR8## (R° is hydrogen or C₁₋₆ alkyl) Y is a non-critical counter anion and representatively is: Cl.sup.⊖, Br.sup.⊖, I.sup.⊖, ##STR9## .sup.⊖ OSO₂ OR°, BF₄.sup.⊖, ClO₄.sup.⊖ and the like; wherein R° is H, Loweralkyl or phenyl;

M.sup.⊕ is H, or an alkali or alkaline earth metal cation such as Na⁺ or K⁺, a tertiary amine salt, or the like;

R² is hydrogen or hydroxyl.

In general words relative to the above reaction diagram, the penicillin starting material (1) or a salt thereof in a solvent such as water at pH 7 to 8, tetrahydrofuran (THF), dimethylformamide (DMF) or the like or aqueous mixtures thereof (ideally such nonaqueous systems contain a base such as triethylamine, methyldiisopropylamine, or the like, to neutralize the acid HX produced by the addition/elimination reaction) is treated with a stoichiometric to four-fold excess of the illustrated electrophilic reagent (2or 3) calculated to provide the desired product. Typically, the reaction is conducted at a temperature of from 0° to 40° C. and is accomplished within 1 to 5 hours. As demonstrated by the following examples, there are no undue criticalities in the parameters of reaction. Starting materials 1 are known: U.S. Pat. No. 3,192,198 (R² =OH); and U.S. Pat. No. 2,985,648 (R² =H).

More specifically, relative to the above reaction scheme, a set of representative conditions may be recited to illustrate a convenient preparation of the compounds of the present invention (I); such recitation, however, is solely for purposes of demonstration and is not to be construed as introducing any undue criticalities of reaction.

Standard Reaction Conditions:

Using a pH meter coupled to an automatic burette containing 1.0 to 2.5 N aqueous sodium hydroxide, a magnetically stirred suspension of the starting material (1) in water is solubilized at pH 7 to pH 7.5 at 20° C.

The heterocyclic reagent (stoichiometric to two-fold excess) is dissolved in water at 20° C. and added to the above solution. Alkali is automatically added to maintain the selected pH in the range 7 to 7.5, the rate of addition being a measure of the extent of reaction. The reaction may also be monitored by removing aliquots at timed intervals for analysis. A particularly suitable analytical scheme is liquid chromatography, for example, high pressure liquid chromatography (HPLC) over a reverse phase column of octadecylsilane (ODS) bonded to silica, using a U.V. detector and aqueous THF (tetrahydrofuran) solution (1 to 30%) as the mobile phase.

The reaction typically takes from 15 minutes to 5 hours at 20° C. The resulting reaction solution at pH 7 is worked up by partition chromatography over a column of Amberlite XAD-2 resin, eluting with aqueous THF solutions (up to 20%) and monitoring the fractions by HPLC as above. However, with the increasing availability of large scale ODS silica columns, the preferred method of product isolation is by preparative reverse phase HPLC directly on the reaction solution at pH 7. The appropriate fractions are combined, evaporated to small volume and lyophilized to yield the product, which is conveniently characterized by IR., U.V., NMR., and analytical HPLC.

In certain cases, the products are sufficiently insoluble in water to separate from the reaction solution at pH 7, and may be isolated simply by filtration.

Finally, a special circumstance should be mentioned. In the basic reaction, first described, the condensation of the penam starting material and the reagent of choice does not occur readily when the group, R, attached directly to the ring nitrogen of the reagent is hydrogen. In such circumstance, it is preferred to employ a quaternized ring nitrogen prior to reaction. The quaternizing group may be removed after the amino heterocycle bond has been formed to yield species of the present invention, I, wherein R is hydrogen: ##STR10## wherein R is --CH₂ OCH₃, --CH₂ OCOCH₃ or the like. According to the above scheme, Ic→Id, the group R is conveniently removed by treating Ic in anhydrous sulpholane at 20° C. with a 3- to 4-fold molar ratio of I Si(CH₃)₃, followed by hydrolysis to yield Id. ##STR11##

IDENTIFICATION OF REAGENTS

The necessary electrophilic, N-heterocyclic reagents 2 and 3 are known and commercially available or may be prepared according to known procedures; see, for example: Advances in Heterocyclic Chemistry, pp. 1-56, Vol. 3 (1964) and pp. 71-121, Vol. 22 (1978); Academic Press. The following list representatively illustrates such reagents. ##STR12## wherein all symbols have previously been defined; the dotted line indicates both saturated and unsaturated rings.

Relative to the above-listed reagents, the preferred values for the radical R which is directly attached to the ring nitrogen atom are: hydrogen; loweralkyl having from 1-10 carbon atoms; substituted alkyl wherein the substituent is chloro, fluoro, hydroxyl, alkoxy, substituted alkoxy, carboxyl, amino, sulfo and mono- and dialkylamino wherein each alkyl has 1-6 carbon atoms; phenylalkyl (alkyl moiety having 1-6 carbon atoms) and substituted phenylalkyl wherein the substituents are selected from chloro, fluoro, carboxyl, amino, hydroxyl, lower alkoxyl having from 1-6 carbon atoms, sulfo, ##STR13## (R° is hydrogen or alkyl having 1-6 carbon atoms). The quinolizinium and indolizinium examples are a special category of preferred values of R, in that R is there an integral part of a bicyclic system (R', defined above).

The preferred values for the other, non-position-specific ring substituent R are: chloro, fluoro, carboxyl and loweralkyl having from 1-6 carbon atoms; substituted lower alkyl wherein the substituent is carboxyl, cyano, alkoxyl having 1-6 carbon atoms, phenyl, and phenyloxy; the preferred value for n is 0 or 1. The preferred leaving group X is chloro or fluoro.

The compounds of the present invention (I) are valuable antibiotics active against various gram-positive and gram-negative bacteria and accordingly find utility in human and veterinary medicine. Representative pathogens which are sensitive to antibiotics I include: Staphyloccus aureus, Escherichia coli, Klebsiella pneumoniae, Bacillus subtilis, Salmonella typhosa, Psuedomonas and Bacterium proteus. The antibacterials of the invention are not limited to utility as medicaments; they may be used in all manner of industry, for example: additives to animal feed, preservation of food, disinfectants, and in other industrial systems where control of bacterial growth is desired. For example, they may be employed in aqueous compositions in concentrations ranging from 0.1 to 100 parts of antibiotic per million parts of solution in order to destroy and inhibit the growth of harmful bacteria on medical and dental equipment and as bactericides in industrial applications, for example in waterbased paints and in the white water of paper mills to inhibit the growth of harmful bacteria.

The products of this invention may be used in any of a variety of pharmaceutical preparations. They may be employed in capsule, powder form, in liquid solution, or in suspension. They may be administered by a variety of means; those of principal interest include: orally, topically or parenterally by injection (intravenously or intramuscularly).

Such tablets and capsules, designed for oral administration, may be in unit dosage form, and may contain conventional excipients, such as binding agents, for example, syrup, acacia, gelatin, sorbitol, tragacanth, or polyvinylpyrrolidone; fillers, for example, lactose, sugar, cornstarch, calcium phosphate, sorbitol, or glycine; lubricants, for example, magnesium stearate, talc, polyethylene glycol, silica; disintegrants, for example, potato starch; or acceptable wetting agents such as sodium lauryl sulphate. The tablets may be coated according to methods well known in the art. Oral liquid preparations may be in the form of aqueous or oily suspensions, or solutions, or they may be presented as a dry product for reconstitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents, for example, sorbitol, methyl cellulose, glucose/sugar syrup, gelatin, hydroxyethylcellulose, or carboxymethyl cellulose. Suppositories will contain conventional suppository bases, such as cocoa butter or other glycerides.

Compositions for injection, the preferred route of delivery, may be prepared in unit dosage form in ampules, or in multidose containers. The compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredient may be in powder form for reconstitution, at the time of delivery, with a suitable vehicle, such as sterile water.

The compositions may also be prepared in suitable forms for absorption through the mucous membranes of the nose and throat or bronchial tissues and may conveniently take the form of liquid sprays or inhalants, lozenges, or throat paints. For medication of the eyes or ears, the preparation may be presented in liquid or semi-solid form. Topical applications may be formulated in hydrophobic or hydrophilic bases as ointments, creams, lotions, paints, or powders.

The dosage to be administered depends to a large extent upon the condition and size of the subject being treated as well as the route and frequency of administration--the parenteral route by injection being preferred for generalized infections. Such matters, however, are left to the routine discretion of the therapist according to principles of treatment well known in the antibiotic art. In general, a daily dosage consists of from about 5 to about 600 mg of active ingredient per kg. of body weight of the subject in one or more treatments per day. A preferred daily dosage for adult humans lies in the range of from about 10 to 240 mg. of active ingredient per kg. of body weight. Another factor influencing the precise dosage regimen, apart from the nature of the infection and peculiar identity of the individual being treated, is the molecular weight of the chosen species of this invention (I).

The compositions for human delivery per unit dosage, whether liquid or solid, may contain from 0.1% to 99% of active material, the preferred range being from about 10-60%. The composition will generally contain from about 15 mg. to about 1500 mg. of the active ingredient; however, in general, it is preferable to employ a dosage amount in the range of from about 250 mg to 1000 mg. In parenteral administration, the unit dosage is usually the pure zwitterionic compound in sterile water solution or in the form of a soluble powder intended for solution. The pH of such solutions typically will correspond to the zwitterionic point; however, consideration of individual properties of solubility and stability may require such aqueous solutions to have a pH other than that of the zwitterionic point, for example in the range of 5.5 to 8.2

The following examples, illustrate but do not limit the product, process, compositional or method of treatment aspects of the present invention. All reaction temperatures are in ° C.

Finally, attention is drawn to a co-pending U.S. Patent application Ser. No. 034,035, of John Hannah which was filed Apr. 27, 1979. Such pending Hannah application is directed to 7-N-heterocyclylcephalosporins which are in analogy to the penicillin compounds of the present invention. Thus, to the extent that the identified application recites common procedures and starting materials, it is hereby incorporated by reference.

EXAMPLE 1 ##STR14## Starting material 1, "ampicillin" (250 mg) was dissolved in distilled, deionized water (4.0 ml) at 22° C., giving a pH of 9.0, which was at once adjusted to pH 7.5 by adding aq. 1.0 N HCl. Reagent 2 4-fluoro-1-methylpyridinium iodide (205 mg; 0.85 mmole) is added. It dissolves with rapid magnetic stirring at 22° C. and drops the pH producing an instant response from the automatic burette set to maintain pH 7.5 by adding aq. 0.5 N NaOH. After 55 minutes, the pH of the pale brown reaction solution is adjusted to 6.0 by adding aq. 1.0 N HCl and the entire solution is put on to a 3×47 cm. column of XAD-2 resin prepared in distilled deionized water eluting with the same solvent.

The eluted fractions are monitored by U.V. absorbance at 254 nm. The elution rate is set at 1 drop per second; and the size of a fraction is set at 300 drops (about 20 ml). At fraction No. 21 the eluting solvent is changed to aqueous 10% THF (tetrahydrofuran) and individual fraction size is reduced to 200 drops (12 ml). Representative fractions are monitored by high pressure liquid chromatography (Water Associates; C₁₈ reverse phase column with aqueous 10% THF as the mobile phase.) Fractions 57-82 are free of starting material 1 and comprise substantially pure product 3; fractions 57-82 are pooled and lyophylized to yield the desired product 3 as a colorless fluffy powder (260 mg);

IR: 1764 cm⁻¹

U.V.: (0.407 mg 3 in 25 ml water): λ_(max) 197 nm: ε28,090; 280 nm: ε23,000.

Following the procedure of Example 1, except substituting an equivalent amount of 2-fluoro-1-methylpyridinium iodide for the 4-fluoro-1-methylpyridinium iodide of Example 1, there is obtained: ##STR15## as an off-white powder; yield: 86%.

I.R.: 1769 cm⁻¹

U.V.: (0.725 mg 4 in 50 ml water): λ_(max) 200 nm: ε31,960; 233 nm: ε13,370; 310 nm; ε8,720;

NMR (T60): δ1.40 (d,J=1 Hz,6H) 4.00 (s, 3H)=N.sup.⊕ --CH₃ ; 4.19 (s, 1H)=H₃ ; 5.47 (s, 2H); 5.60 (s, 1H)=H₅, H₆, H₁₀ ; 7.50 (s, 5H)=C₆ H₅ ; 6.92-8.12 (m, 4H)= ##STR16##

EXAMPLE 2

Following the procedure described in the foregoing text and Examples, the following compounds listed in Table I are obtained. In Table I, appropriate remarks are entered to signal any departure from established procedure. Also listed under "Remarks" in Table I are the necessary reagents.

                                      TABLE I                                      __________________________________________________________________________      ##STR17##                                                                     Compound                                                                             R.sup.2                                                                              R'                       Remark's                                  __________________________________________________________________________     1     H                                                                                  ##STR18##                                                                                               ##STR19##                                   2     H                                                                                  ##STR20##                                                                                               ##STR21##                                   3     H                                                                                  ##STR22##                                                                                               ##STR23##                                   4     H                                                                                  ##STR24##                                                                                               ##STR25##                                   5     H                                                                                  ##STR26##                                                                                               ##STR27##                                   6     H                                                                                  ##STR28##                                                                                               ##STR29##                                   7     H                                                                                  ##STR30##                                                                                               ##STR31##                                   8     H                                                                                  ##STR32##               From Compound 7 by reaction with (a)                                           ISi(CH.sub. 3).sub.3 then (b) H.sub.2                                          O.                                           9     H                                                                                  ##STR33##                                                                                               ##STR34##                                   10    H                                                                                  ##STR35##               from compound 9 by hydrolysis at pH = 9                                        hen titration to pH = 7                      11    H                                                                                  ##STR36##                                                                                               ##STR37##                                   12    H                                                                                  ##STR38##               from compound 11 by hydrolysis at pH =                                         9 then titration to pH = 7                   13    H                                                                                  ##STR39##                                                                                               ##STR40##                                   14    H                                                                                  ##STR41##               from compound 13 by hydrolysis at pH =                                         9 then titration at pH = 7                   15    H                                                                                  ##STR42##                                                                                               ##STR43##                                   16    H                                                                                  ##STR44##                                                                                               ##STR45##                                   17    H                                                                                  ##STR46##                                                                                               ##STR47##                                   18    H                                                                                  ##STR48##                                                                                               ##STR49##                                   19    H                                                                                  ##STR50##                                                                                               ##STR51##                                   20    H                                                                                  ##STR52##                                                                                               ##STR53##                                   21    H                                                                                  ##STR54##               from compound 8 . by reaction with                                             H.sub.2 N . O . SO.sub.3 H                   22    H                                                                                  ##STR55##                                                                                               ##STR56##                                                                     and subsequent hydrolysis                                                      at pH = 9 and titration to                                                     pH = 7                                       23    H                                                                                  ##STR57##                                                                                               ##STR58##                                                                     and subsequent cleavage                                                        by CF.sub. 3 COOH                            24    H                                                                                  ##STR59##                                                                                               ##STR60##                                                                     and subsequent cleavage                                                        by CF.sub.3 COOH                             25    H                                                                                  ##STR61##               from compound 16 by reaction with (a)                                          ISi(CH.sub.3).sub.3 then (b)H.sub.2 O        26    H                                                                                  ##STR62##                                                                                               ##STR63##                                   27    H                                                                                  ##STR64##               from compound 26 by reaction with                                              (a)ISi(CH.sub.3).sub.3 ; (b)H.sub.2 O;                                         then M.sup.⊕ OH.sup.⊖  to                                          pH 7 isolating the product as the                                              cephem COO.sup.⊖ M.sup.⊕         28    H                                                                                  ##STR65##                                                                                               ##STR66##                                   29    H                                                                                  ##STR67##                                                                                               ##STR68##                                   30    H                                                                                  ##STR69##                                                                                               ##STR70##                                   31    H                                                                                  ##STR71##                                                                                               ##STR72##                                   32    H                                                                                  ##STR73##                                                                                               ##STR74##                                   33    H                                                                                  ##STR75##                                                                                               ##STR76##                                   34    H                                                                                  ##STR77##                                                                                               ##STR78##                                   35    H                                                                                  ##STR79##                                                                                               ##STR80##                                   36    H                                                                                  ##STR81##               from compound 35 by hydrolysis at pH 9.                                        hen titration to pH 7                        37    H                                                                                  ##STR82##                                                                                               ##STR83##                                                                     and subsequent hydrolysis                                                      at pH = 9 and titration to                                                     pH = 7                                       38    OH                                                                                 ##STR84##               from compound 34 by reaction with (a)                                          LiOCH.sub.3 then (b)ClOBu.sup.t              39    OH                                                                                 ##STR85##               from compound 18 by reaction with                                              LiOCH.sub.3 then (b) ClOBu.sup.t             40    H                                                                                  ##STR86##                                                                                               ##STR87##                                                                     and subsequent hydrolysis at                                                   pH 9 and titration to pH 7                   41    H                                                                                  ##STR88##                                                                                               ##STR89##                                   42    H                                                                                  ##STR90##                                                                                               ##STR91##                                   43    H                                                                                  ##STR92##               from compound 42 by hydrolysis at pH 9                                         then titration to pH 7                       44    H                                                                                  ##STR93##                                                                                               ##STR94##                                   45    H                                                                                  ##STR95##                                                                                               ##STR96##                                   46    H                                                                                  ##STR97##                                                                                               ##STR98##                                                                     by reaction in anhydrous DMF                                                   with diethylisopropylamine as                                                  base                                         47    H                                                                                  ##STR99##                                                                                               ##STR100##                                  48    H                                                                                  ##STR101##              from compound 47 by hydro- lysis at pH                                         9 then titration to pH 7                     49    H                                                                                  ##STR102##                                                                                              ##STR103##                                  50    H                                                                                  ##STR104##              from compound 49 by hydrolysis at pH 9                                         then titration to pH 7                       51    H                                                                                  ##STR105##                                                                                              ##STR106##                                  52    H                                                                                  ##STR107##                                                                                              ##STR108##                                  53    H                                                                                  ##STR109##                                                                                              ##STR110##                                  54    H                                                                                  ##STR111##                                                                                              ##STR112##                                  55    H                                                                                  ##STR113##                                                                                              ##STR114##                                  56    H                                                                                  ##STR115##              from compound 55 by reaction with (a)                                          ISi(CH.sub.3).sub.3 then (b) H.sub.2 O       57    H                                                                                  ##STR116##                                                                                              ##STR117##                                  58    H                                                                                  ##STR118##                                                                                              ##STR119##                                  59    H                                                                                  ##STR120##              from compound 56 by reaction with                                              H.sub.2 NO . SO.sub.3 H                      60    H                                                                                  ##STR121##                                                                                              ##STR122##                                  61    H                                                                                  ##STR123##              from compound 60 by hydrolysis at pH 9                                         then titration to pH 7                       62    H                                                                                  ##STR124##                                                                                              ##STR125##                                                                    and subsequent cleavage by                                                     CF.sub.3 . COOH                              63    H                                                                                  ##STR126##                                                                                              ##STR127##                                                                    and subsequent                                                                 hydrolysis at pH 9                                                             and titration to pH 7                        64    H                                                                                  ##STR128##                                                                                              ##STR129##                                  65    H                                                                                  ##STR130##                                                                                              ##STR131##                                                                    and subsequent hydrolysis at                                                   pH 9 titration to pH 7                       66    H                                                                                  ##STR132##                                                                                              ##STR133##                                  67    H                                                                                  ##STR134##              from compound 66 by hydro- lysis at pH                                         9 then titration to pH 7                     68    H                                                                                  ##STR135##                                                                                              ##STR136##                                  69    OH                                                                                 ##STR137##                                                           70    OH                                                                                 ##STR138##                                                           71    H                                                                                  ##STR139##                                                                                              ##STR140##                                  72    H                                                                                  ##STR141##                                                                                              ##STR142##                                  73    H                                                                                  ##STR143##                                                                                              ##STR144##                                  74    H                                                                                  ##STR145##              from compound 73 by hydro- lysis at pH                                         9 then titration to pH 7                     75    H                                                                                  ##STR146##                                                                                              ##STR147##                                  76    H                                                                                  ##STR148##              from compound 75 by hydrolysis at pH 9                                         then titration to pH 7                       77    H                                                                                  ##STR149##                                                                                              ##STR150##                                  78    OH                                                                                 ##STR151##                                                           79    H                                                                                  ##STR152##                                                                                              ##STR153##                                  80    H                                                                                  ##STR154##                                                                                              ##STR155##                                  81    H                                                                                  ##STR156##                                                                                              ##STR157##                                  82    H                                                                                  ##STR158##                                                                                              ##STR159##                                  83    H                                                                                  ##STR160##                                                                                              ##STR161##                                  84    OH                                                                                 ##STR162##                                                           85    H                                                                                  ##STR163##                                                                                              ##STR164##                                  86    H                                                                                  ##STR165##                                                                                              ##STR166##                                  87    H                                                                                  ##STR167##                                                                                              ##STR168##                                  88    OH                                                                                 ##STR169##                                                           89    H                                                                                  ##STR170##                                                                                              ##STR171##                                  90    H                                                                                  ##STR172##                                                                                              ##STR173##                                  91    H                                                                                  ##STR174##                                                                                              ##STR175##                                  92    H                                                                                  ##STR176##                                                                                              ##STR177##                                  93    H                                                                                  ##STR178##                                                                                              ##STR179##                                  94    H                                                                                  ##STR180##              from compound 93 by hydro- lysis at pH                                         9 then titration to pH 7                     95    H                                                                                  ##STR181##                                                                                              ##STR182##                                  96    OH                                                                                 ##STR183##                                                           97    H                                                                                  ##STR184##                                                                                              ##STR185##                                  98    H                                                                                  ##STR186##                                                                                              ##STR187##                                  99    H                                                                                  ##STR188##                                                                                              ##STR189##                                  100   H                                                                                  ##STR190##                                                                                              ##STR191##                                  101   H                                                                                  ##STR192##                                                                                              ##STR193##                                  102   H                                                                                  ##STR194##                                                                                              ##STR195##                                  103   H                                                                                  ##STR196##                                                                                              ##STR197##                                  104   H                                                                                  ##STR198##                                                                                              ##STR199##                                  105   H                                                                                  ##STR200##                                                                                              ##STR201##                                  106   H                                                                                  ##STR202##                                                                                              ##STR203##                                  107   OH                                                                                 ##STR204##                                                           108   H                                                                                  ##STR205##                                                                                              ##STR206##                                  109   H                                                                                  ##STR207##              prepared from compound 108 by reaction                                         with (a) ISi(CH.sub.3).sub.3 then (b)                                          H.sub.2 O                                    110   H                                                                                  ##STR208##                                                                                              ##STR209##                                  111   H                                                                                  ##STR210##                                                                                              ##STR211##                                  112   H                                                                                  ##STR212##                                                                                              ##STR213##                                  113   H                                                                                  ##STR214##                                                                                              ##STR215##                                  114   H                                                                                  ##STR216##                                                                                              ##STR217##                                  115   H                                                                                  ##STR218##                                                                                              ##STR219##                                  __________________________________________________________________________

EXAMPLE 3 ##STR220## Preparation of Pharmaceutical Compositions

One such unit dosage form comprises a blend of 120 mg of 1 with 20 mg of lactose and 5 mg of magnesium stearate which is placed in a No. 3 gelatin capsule. Similarly, by employing more of the active ingredient and less lactose, other dosage forms can be prepared; should it be necessary to mix more than 145 mg. of ingredients together, larger capsules may be employed. Equivalently, compressed tablets and pills can be prepared. The following examples are further illustrative of the preparation of pharmaceutical formulations:

    ______________________________________                                         TABLET           PER TABLET                                                    ______________________________________                                         Compound 1 ˜                                                                              125 mg.                                                       Dicalcium Phosphate                                                                             200 mg.                                                       Cornstarch, U.S.P.                                                                               6 mg.                                                        Lactose, U.S.P.  200 mg.                                                       Magnesium Stearate                                                                              270 mg.                                                       ______________________________________                                    

The above ingredients are combined and the mixture is compressed into tablets, approximately 0.5 inch in diameter each weighing 800 mg. 

What is claimed is
 1. A compound having the structural formula: ##STR221## and the pharmaceutically acceptable salts and esters thereof wherein: R² is hydrogen or hydroxyl; andR' is selected from the group consisting of: ##STR222## wherein the dotted line indicates both saturated and unsaturated rings; andwherein: R is alkyl having from 1-6 carbon atoms, substituted alkyl having from 1-6 carbon atoms wherein the substituent is chloro, fluoro, hydroxyl, alkoxyl (C₁₋₆), carboxyl, amino, sulfo and mono- and dialkylamino wherein each alkyl has 1-6 carbon atoms substituted and unsubstituted phenylalkyl and phenylalkenyl having 7-12 carbon atoms wherein the substituent is selected from chloro, fluoro, carboxyl, amino, cyano, hydroxyl and sulfo; R³ is chloro, fluoro, hydroxyl, carboxyl, sulfo, cyano, amino, mono- and dialkylamino, alkoxyl, alkyl having from 1-6 carbon atoms, substituted alkyl having 1-6 carbon atoms wherein the substituent is carboxyl, cyano, alkoxyl having 1-6 carbon atoms, phenyl and phenyloxy; n is an integer selected from 0 to
 3. 2. A compound according to claim 1 wherein n is 0 or 1; and R is hydrogen or substituted or unsubstituted alkyl or phenylalkyl.
 3. A compound according to claim 2 wherein R' is selected from the group consisting of:

    __________________________________________________________________________      ##STR223##                                                                                         ##STR224##                                                 ##STR225##                                                                                         ##STR226##                                                 ##STR227##                                                                                         ##STR228##                                                 ##STR229##                                                                                         ##STR230##                                                 ##STR231##                                                                     ##STR232##                                                                                         ##STR233##                                                 ##STR234##                                                                                         ##STR235##                                                 ##STR236##                                                                                         ##STR237##                                                 ##STR238##                                                                                         ##STR239##                                                 ##STR240##                                                                                         ##STR241##                                                 ##STR242##                                                                                         ##STR243##                                                 ##STR244##                                                                                         ##STR245##                                                 ##STR246##                                                                                         ##STR247##                                                 ##STR248##                                                                                         ##STR249##                                                 ##STR250##                                                                                         ##STR251##                                                 ##STR252##                                                                                         ##STR253##                                                 ##STR254##                                                                                         ##STR255##                                                 ##STR256##                                                                                         ##STR257##                                                 ##STR258##                                                                                         ##STR259##                                                 ##STR260##                                                                                         ##STR261##                                                 ##STR262##                                                                                         ##STR263##                                                 ##STR264##                                                                     ##STR265##                                                                                         ##STR266##                                                 ##STR267##                                                                                         ##STR268##                                                 ##STR269##                                                                                         ##STR270##                                                                     ##STR271##                                                 ##STR272##                                                                                         ##STR273##                                                 ##STR274##                                                                                         ##STR275##                                                 ##STR276##                                                                                         ##STR277##                                                 ##STR278##                                                                                         ##STR279##                                                 ##STR280##                                                                                         ##STR281##                                                 ##STR282##                                                                                         ##STR283##                                                 ##STR284##                                                                                         ##STR285##                                                 ##STR286##                                                                                         ##STR287##                                                 ##STR288##                                                                                         ##STR289##                                                 ##STR290##                                                                                         ##STR291##                                                 ##STR292##                                                                                         ##STR293##                                                 ##STR294##                                                                                         ##STR295##                                                 ##STR296##                                                                                         ##STR297##                                                 ##STR298##                                                                     ##STR299##                                                                                         ##STR300##                                                 ##STR301##                                                                                         ##STR302##                                                 ##STR303##                                                                     ##STR304##                                                                                         ##STR305##                                                 ##STR306##                                                                                         ##STR307##                                                 ##STR308##                                                                                         ##STR309##                                                 ##STR310##                                                                                         ##STR311##                                                 ##STR312##                                                                                         ##STR313##                                                 ##STR314##                                                                                         ##STR315##                                                 ##STR316##                                                                                         ##STR317##                                                 ##STR318##                                                                                         ##STR319##                                                 ##STR320##                                                                                         ##STR321##                                                 ##STR322##                                                                                         ##STR323##                                                                     ##STR324##                                                 ##STR325##                                                                                         ##STR326##                                                 ##STR327##                                                                                         ##STR328##                                                __________________________________________________________________________

wherein M is hydrogen or a pharmaceutically acceptable cation.
 4. An antibacterial pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 1 and a pharmaceutical carrier therefor. 